rs2032582 is a genetic variant on gene ABCB1 associated with Inflammatory bowel disease 13.
rs10876864 is a genetic variant on gene IKZF4 associated with Intelligence and Allergic disease.
rs11540652 is a genetic variant on gene TP53 associated with Li-fraumeni syndrome 1 and Multiple myeloma.
rs104894226 is a genetic variant on gene HRAS associated with Costello syndrome and Large congenital melanocytic nevus.
rs7274581 is a genetic variant associated with Alzheimer's disease.
rs10808546 is a genetic variant associated with Abdominal aortic aneurysm.
is a rare genetic condition causing a small head and eye damage.
is a rare genetic condition causing a small head and vision problems.
is a genetic disorder causing small head size, albinism, and hand anomalies.
is a genetic syndrome with small head size, short fingers, and scoliosis.
is a genetic disorder causing small head size, brain problems, and spasticity.
is a rare genetic disorder causing small head size and capillary changes.
is a rare genetic syndrome affecting brain growth, heart, and lung development.
is a rare genetic condition causing a small head and cardiomyopathy.
is a rare genetic disorder affecting brain growth, balance, and heart rhythm.
is a rare genetic condition causing small head and fused neck bones.
is a rare genetic condition with microcephaly, cleft palate, and retinal changes.
is a rare genetic condition causing small head size and nerve damage.
is a genetic syndrome causing small head size, cataracts, and skin rash.
is a rare genetic condition affecting brain development, facial features, and learning.
is a rare genetic condition affecting brain growth, development, and facial features.
is a rare genetic condition causing microcephaly, hearing loss, and intellectual disability.
is a rare genetic disorder causing small head and facial, eye abnormalities.
is a genetic disorder causing small head, facial, heart, and skeletal differences.
is a rare genetic syndrome with small head, kidney disease, marfanoid features.
is a syndrome with microcephaly, intellectual disability, seizures, hearing loss, abnormal tone.
is a rare genetic condition affecting brain growth, vision, and lymphatic swelling.
is a rare genetic condition causing a small head and small eyes.
is a rare genetic condition causing a small head and short limbs.
is a rare genetic disorder affecting brain development and head growth.